aducanumab
Sign in to saveAlso known as BIIB-037, BART, BIIB037, Aduhelm
Aducanumab, sold under the brand name Aduhelm, is an anti-amyloid drug designed to treat Alzheimer's disease. It is a monoclonal antibody that targets aggregated forms (plaque) of amyloid beta (Aβ) found in the brains of people with Alzheimer's disease to reduce its buildup. It was developed by Biogen and Eisai. Aducanumab is given via intravenous infusion.
Key facts
- Drug.type
- mab
- Drug.mab_type
- mab
- Drug.source
- u
- Drug.target
- Amyloid beta
- Drug.tradename
- Aduhelm
- Drug.DailyMedID
- Aducanumab
- Drug.routes_of_administration
- Intravenous
- Drug.ATC_prefix
- N06
- Drug.ATC_suffix
- DX03
- Drug.legal_US
- Rx-only
- Drug.elimination_half life
- 24.8 days
- Drug.CAS_number
- 1384260-65-4
- Drug.DrugBank
- DB12274
- Drug.ChemSpiderID
- none
- Drug.UNII
- 105J35OE21
- Drug.KEGG
- D10541
- Drug.synonyms
- Aducanumab-avwa, BIIB037, BIIB-037
- Drug.C
- 6472
via Wikipedia infobox
~14 min read
Encyclopedic overview
17 sectionsContents
- Medical uses
- Mechanism of action
- Adverse effects
- History
- Clinical trials
- FDA review and approval
- Coverage in the United States
- European review
- Abandonment
- Society and culture
- Efficacy
- Process concerns
- Economics and cost
- Sales
- Names
- References
- External links
Aducanumab, sold under the brand name Aduhelm, is an anti-amyloid drug designed to treat Alzheimer's disease. It is a monoclonal antibody that targets aggregated forms (plaque) of amyloid beta (Aβ) found in the brains of people with Alzheimer's disease to reduce its buildup. It was developed by Biogen and Eisai. Aducanumab is given via intravenous infusion.
Aducanumab was approved for medical use in the United States by the Food and Drug Administration (FDA) in June 2021, in a controversial decision that led to the resignation of three advisers to the FDA in the absence of evidence that the medication is effective. The FDA stated that it represents a first-of-its-kind treatment approved for Alzheimer's disease and that it is the first new treatment approved for Alzheimer's since 2003. Aducanumab's approval is controversial for numerous reasons including ambiguous clinical trial results regarding efficacy, the high cost of the medication and the very high rate of serious adverse events. The FDA considers it to be a first-in-class medication.
Excerpted from Wikipedia’s “aducanumab” article, available under the CC BY-SA 4.0 licence.